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Study identifier: NCT06826196 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of ALD-102 Solution in Subjects With Alopecia Areata

Condition: Alopecia Areata (AA)  ·  Sponsor: Aldena Therapeutics

PhasePhase 1/Phase 2
Planned participants24
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersNo

About this study

The goal of this first-in-human clinical trial is to learn if ALD-102 Solution is safe and well tolerated following injections in the scalp in subjects with alopecia areata. The study will also learn about the effect of ALD-102 on hair regrowth in treatment areas. The researchers will compare the effects of ALD-102 Solution (drug) to placebo (saline solution that contains no drug) or an untreated area. Study participants will have treatment areas selected on the scalp to receive ALD-102 Solution (drug), placebo (saline solution) or to remain untreated. Injections will occur once every 4 weeks for a treatment period of 8 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Chief Scientific Officer  ·  +44 2045915017  ·  info@aldenatherapeutics.com

Always discuss trial participation with your own doctor first.

Locations (7)

Clinical Trial Research InstituteThousand Oaks, California, United StatesRecruiting
Options Research GroupWest Lafayette, Indiana, United StatesRecruiting
The Brigham and Women's HospitalBoston, Massachusetts, United StatesRecruiting
Dermatology Specialists of SpokaneSpokane, Washington, United StatesRecruiting
The Centre for Clinical TrialsOakville, Ontario, CanadaRecruiting
InnovadermMontreal, Quebec, CanadaRecruiting
Centre de Recherche Saint-LouisQuébec, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06826196